MEDNETIC (UDI 08681645053945)
Manufactured by TECHNOCAST OTOMOTİV SANAYİ VE TİC. A.Ş. MEDİKAL ŞUBESİ
Device Regulatory Overview
The MEDNETIC (Model/Catalog Number: PG.BS.10.18/21.8.A) is a medical device manufactured by TECHNOCAST OTOMOTİV SANAYİ VE TİC. A.Ş. MEDİKAL ŞUBESİ. This product is indexed under FDA Product Code / Category Classification G03040301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PG.BS.10.18/21.8.A
- Product Code / EMDN
- G03040301
- Device Name
- 10F 180/200cm Biliary Stent Set, 8cm Stent Ams
- Database Sync Date
- 2026-08-09 16:28:44
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MEDNETIC?
The registered manufacturer of record for MEDNETIC is TECHNOCAST OTOMOTİV SANAYİ VE TİC. A.Ş. MEDİKAL ŞUBESİ.
What is the Primary UDI-DI identifier for MEDNETIC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681645053945.
What classification code is assigned to this device?
This device is registered under product classification code G03040301.
Similar Classification Devices (G03040301)
Other Devices by TECHNOCAST OTOMOTİV SANAYİ VE TİC. A.Ş. MEDİKAL ŞUBESİ
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